drugset / Trial / NCT04529096

Chronic Pain Master Protocol (CPMP): A Study of LY3016859 in Participants With Chronic Low Back Pain

NCT04529096 ↗

Phase 2 Completed 149 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is being done to test the safety and efficacy of the study drug LY3016859 for the treatment of chronic low back pain. This trial is part of the chronic pain master protocol H0P-MC-CPMP (NCT05986292) which is a protocol to accelerate the development of new treatments for chronic pain.

Timeline

Start
2020-08-25
Primary completion
2021-06-04
Completion
2021-10-04

Outcome

Missed primary endpoint

registry analysis (superiority test); 750 Mg-500 mg LY3016859 vs Placebo; Posterior Mean Difference 0.52 (95% CI -0.10 to 1.14); Bayesian Mixed Model Analysis NCT04529096 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Fepixnebart Monoclonal antibody 500 mg Intravenous

Indications